Metal−Organic Anion Receptors:  Arranging Urea Hydrogen-Bond Donors to Encapsulate Sulfate Ions

2004 ◽  
Vol 126 (16) ◽  
pp. 5030-5031 ◽  
Author(s):  
Chantelle R. Bondy ◽  
Philip A. Gale ◽  
Stephen J. Loeb
2008 ◽  
pp. 5695 ◽  
Author(s):  
Matthew G. Fisher ◽  
Philip A. Gale ◽  
Mark E. Light ◽  
Stephen J. Loeb

2019 ◽  
Vol 48 (27) ◽  
pp. 10199-10209 ◽  
Author(s):  
Ming-Yu Zhao ◽  
Jian-Nan Zhu ◽  
Peng Li ◽  
Wei Li ◽  
Ting Cai ◽  
...  

Seven transition metal–organic frameworks with structures ranging from one-dimensional chains to three-dimensional networks have been synthesized in deep eutectic solvents.


2014 ◽  
Vol 43 (17) ◽  
pp. 6198-6213 ◽  
Author(s):  
Jiajia Cai ◽  
Jonathan L. Sessler

Neutral and cationic CH hydrogen bond donors have been actively used in various shape persistent macrocycles, foldamers and “molecular machines”.


Author(s):  
Hong-Bo Wang ◽  
James A Wisner ◽  
Michael C Jennings

The synthesis, X-ray crystal structures and anion recognition properties of two receptors containing thiazine-1,1-dioxide heterocycles as hydrogen bond donating subunits are reported. The newly synthesized receptors display much different anion selectivities in acetone-d 6 than N,N′-diphenyl-1,3-disulfonamidobenzene that was used as a comparison. The selectivity exhibited by one of the new receptors for chloride anions can be attributed to greater steric demand in the cleft formed, in part, by its terminal phenyl rings; an effect that is absent in the comparison receptor.


2013 ◽  
Vol 117 (39) ◽  
pp. 19991-20001 ◽  
Author(s):  
Julia Wack ◽  
Renée Siegel ◽  
Tim Ahnfeldt ◽  
Norbert Stock ◽  
Luís Mafra ◽  
...  

2014 ◽  
Vol 67 (23-24) ◽  
pp. 3863-3872 ◽  
Author(s):  
Andrea Ienco ◽  
Maria Caporali ◽  
Ferdinando Costantino ◽  
Annalisa Guerri ◽  
Gabriele Manca ◽  
...  

2017 ◽  
Vol 46 (15) ◽  
pp. 4960-4967 ◽  
Author(s):  
Ferdinand Groenewald ◽  
Helgard G. Raubenheimer ◽  
Jan Dillen ◽  
Catharine Esterhuysen

MP2/aug-cc-pVTZ-pp calculations show that the Au(i) atom of dimethylaurate behaves as a hydrogen-bond acceptor to a range of hydrogen-bond donors.


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